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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395207Generated: October 31, 2026

3,5-Dimethylpiperidine → HCID 57263213, compound

https://huagongshe.com/reaction/1395207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DimethylpiperidineHCID 118259—
ReactantHCID 57148770HCID 57148770—
SolventDiethyl EtherHCID 3283—
ProductHCID 57263213HCID 57263213—

Reaction Steps

62 G. of 3-(p-tert.-amyl-phenyl)-2,3-dimethyl-allyl bromide in 150 ml. of ether are added dropwise to a solution of 45.2 g. of 3,5-dimethylpiperidine in 200 ml. of absolute ether and the mixture is heated at reflux for 16 hours. The 3,5-dimethylpiperidine hydrobromide is removed by filtration and back-washed with ether. The ether solution is extracted with 2 N hydrochloric acid and made alkaline with 50% sodium hydroxide. The alkaline-aqueous solution is again extracted with ether, washed with water, dried over sodium sulfate and evaporated. By distillation, there is obtained pure 1-[3-(p-tert.-amylphenyl)-2,3-dimethyl-2-propenyl]-3,5-dimethylpiperidine having a boiling point of 155° C./0.04 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202894
Source datasetuspto-grants-1980_05
ORD IDord-75d8975e17d446a991804938251707f8
Source noteuspto-grants-1980_05